| pubmed-article:6620324 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:6620324 | lifeskim:mentions | umls-concept:C0917713 | lld:lifeskim |
| pubmed-article:6620324 | lifeskim:mentions | umls-concept:C0426857 | lld:lifeskim |
| pubmed-article:6620324 | lifeskim:mentions | umls-concept:C0043292 | lld:lifeskim |
| pubmed-article:6620324 | lifeskim:mentions | umls-concept:C0023745 | lld:lifeskim |
| pubmed-article:6620324 | lifeskim:mentions | umls-concept:C0162326 | lld:lifeskim |
| pubmed-article:6620324 | lifeskim:mentions | umls-concept:C1882417 | lld:lifeskim |
| pubmed-article:6620324 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:6620324 | pubmed:dateCreated | 1983-11-23 | lld:pubmed |
| pubmed-article:6620324 | pubmed:abstractText | A study of DNA restriction fragment polymorphisms and Becker muscular dystrophy has shown eight families informative for the cloned sequence L1.28, which is located on the short arm of the X chromosome between Xp110 and Xp113. Analysis of these families reveals linkage between the two loci, with the maximum likelihood estimate of the genetic distance being 16 centiMorgans (95% confidence limits between 7 and 32 centiMorgans). Since a study of DNA polymorphisms in Duchenne muscular dystrophy has shown a comparable linkage distance with L1.28, our results suggest that the locus for Becker muscular dystrophy, like that for Duchenne dystrophy, is on the short arm of the X chromosome, and further that these two loci may be closely linked or possibly allelic. | lld:pubmed |
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| pubmed-article:6620324 | pubmed:language | eng | lld:pubmed |
| pubmed-article:6620324 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:6620324 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:6620324 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:6620324 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:6620324 | pubmed:issn | 0022-2593 | lld:pubmed |
| pubmed-article:6620324 | pubmed:author | pubmed-author:HarperP SPS | lld:pubmed |
| pubmed-article:6620324 | pubmed:author | pubmed-author:PearsonP LPL | lld:pubmed |
| pubmed-article:6620324 | pubmed:author | pubmed-author:ThomasN SNS | lld:pubmed |
| pubmed-article:6620324 | pubmed:author | pubmed-author:KingstonH MHM | lld:pubmed |
| pubmed-article:6620324 | pubmed:author | pubmed-author:SarfaraziMM | lld:pubmed |
| pubmed-article:6620324 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:6620324 | pubmed:volume | 20 | lld:pubmed |
| pubmed-article:6620324 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:6620324 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:6620324 | pubmed:pagination | 255-8 | lld:pubmed |
| pubmed-article:6620324 | pubmed:dateRevised | 2010-11-18 | lld:pubmed |
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| pubmed-article:6620324 | pubmed:meshHeading | pubmed-meshheading:6620324-... | lld:pubmed |
| pubmed-article:6620324 | pubmed:year | 1983 | lld:pubmed |
| pubmed-article:6620324 | pubmed:articleTitle | Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome. | lld:pubmed |
| pubmed-article:6620324 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:6620324 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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